scholarly article | Q13442814 |
P819 | ADS bibcode | 2017NatCo...815293C |
P6179 | Dimensions Publication ID | 1085378079 |
P356 | DOI | 10.1038/NCOMMS15293 |
P932 | PMC publication ID | 5436228 |
P698 | PubMed publication ID | 28489077 |
P50 | author | Marcial Camacho-Perez | Q56904059 |
Thorsten Trimbuch | Q56960887 | ||
Christian Rosenmund | Q33274633 | ||
P2093 | author name string | Josep Rizo | |
Shwu-Shin Chang | |||
Jayeeta Basu | |||
Masin Abo-Rady | |||
Cristina Pulido-Lozano | |||
Irina Duluvova | |||
Shuwen Chang | |||
P2860 | cites work | Tomosyn inhibits synaptic vesicle priming in Caenorhabditis elegans | Q21563608 |
RIM determines Ca²+ channel density and vesicle docking at the presynaptic active zone | Q26269881 | ||
Munc13 C2B domain is an activity-dependent Ca2+ regulator of synaptic exocytosis | Q26269911 | ||
RIM proteins activate vesicle priming by reversing autoinhibitory homodimerization of Munc13 | Q26269920 | ||
RIM proteins tether Ca2+ channels to presynaptic active zones via a direct PDZ-domain interaction | Q26269921 | ||
Structural basis for a Munc13-1 homodimer to Munc13-1/RIM heterodimer switch | Q26269950 | ||
A Munc13/RIM/Rab3 tripartite complex: from priming to plasticity? | Q26269969 | ||
Open syntaxin docks synaptic vesicles | Q27334556 | ||
Munc13-1 is essential for fusion competence of glutamatergic synaptic vesicles | Q27863297 | ||
Drosophila UNC-13 is essential for synaptic transmission | Q28145978 | ||
Functional interaction of the active zone proteins Munc13-1 and RIM1 in synaptic vesicle priming | Q28188061 | ||
RIM1alpha forms a protein scaffold for regulating neurotransmitter release at the active zone | Q28215837 | ||
Total arrest of spontaneous and evoked synaptic transmission but normal synaptogenesis in the absence of Munc13-mediated vesicle priming | Q28504670 | ||
The morphological and molecular nature of synaptic vesicle priming at presynaptic active zones | Q28506683 | ||
Beta phorbol ester- and diacylglycerol-induced augmentation of transmitter release is mediated by Munc13s and not by PKCs | Q28511979 | ||
A common molecular basis for membrane docking and functional priming of synaptic vesicles | Q28512083 | ||
Identification of the minimal protein domain required for priming activity of Munc13-1. | Q50748500 | ||
Calmodulin and Munc13 Form a Ca2+ Sensor/Effector Complex that Controls Short-Term Synaptic Plasticity | Q58191207 | ||
Phorbol esters modulate spontaneous and Ca2+-evoked transmitter release via acting on both Munc13 and protein kinase C | Q81781158 | ||
Munc13 mediates the transition from the closed syntaxin-Munc18 complex to the SNARE complex | Q28569612 | ||
Differential expression of two novel Munc13 proteins in rat brain | Q28572369 | ||
Rim is a putative Rab3 effector in regulating synaptic-vesicle fusion | Q28575529 | ||
Differential control of vesicle priming and short-term plasticity by Munc13 isoforms | Q28592163 | ||
Germline transmission and tissue-specific expression of transgenes delivered by lentiviral vectors | Q29547596 | ||
Definition of the readily releasable pool of vesicles at hippocampal synapses | Q29620402 | ||
Vps4 disassembles an ESCRT-III filament by global unfolding and processive translocation | Q35685098 | ||
Syntaxin opening by the MUN domain underlies the function of Munc13 in synaptic-vesicle priming | Q36734003 | ||
Liprin-α2 promotes the presynaptic recruitment and turnover of RIM1/CASK to facilitate synaptic transmission | Q36917565 | ||
Functional synergy between the Munc13 C-terminal C1 and C2 domains | Q37052784 | ||
Reconstitution of the vital functions of Munc18 and Munc13 in neurotransmitter release | Q37071048 | ||
ELKS controls the pool of readily releasable vesicles at excitatory synapses through its N-terminal coiled-coil domains. | Q37071725 | ||
Position of UNC-13 in the active zone regulates synaptic vesicle release probability and release kinetics | Q37290090 | ||
UNC-13 and UNC-10/rim localize synaptic vesicles to specific membrane domains. | Q37417587 | ||
Excitatory and inhibitory autaptic currents in isolated hippocampal neurons maintained in cell culture | Q37588622 | ||
Ultrafast endocytosis at mouse hippocampal synapses. | Q37642826 | ||
UNC-13 interaction with syntaxin is required for synaptic transmission. | Q38319125 | ||
CAPS-1 and CAPS-2 are essential synaptic vesicle priming proteins. | Q39752415 | ||
Munc13-1 is a presynaptic phorbol ester receptor that enhances neurotransmitter release | Q41017986 | ||
An open form of syntaxin bypasses the requirement for UNC-13 in vesicle priming | Q41768196 | ||
Munc13-1 C1 domain activation lowers the energy barrier for synaptic vesicle fusion. | Q42507707 | ||
Vesicle priming and recruitment by ubMunc13-2 are differentially regulated by calcium and calmodulin | Q42524920 | ||
UNC-13 is required for synaptic vesicle fusion in C. elegans | Q43240851 | ||
Direct interactions between C. elegans RAB-3 and Rim provide a mechanism to target vesicles to the presynaptic density | Q43241214 | ||
Binding to Rab3A-interacting molecule RIM regulates the presynaptic recruitment of Munc13-1 and ubMunc13-2. | Q45345777 | ||
A minimal domain responsible for Munc13 activity | Q46755751 | ||
A complete genetic analysis of neuronal Rab3 function. | Q47952687 | ||
Dynamic control of synaptic vesicle replenishment and short-term plasticity by Ca(2+)-calmodulin-Munc13-1 signaling | Q48461386 | ||
The effects of temperature on vesicular supply and release in autaptic cultures of rat and mouse hippocampal neurons | Q48667536 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P4510 | describes a project that uses | ImageJ | Q1659584 |
P407 | language of work or name | English | Q1860 |
P921 | main subject | protein heterodimerization activity | Q14762999 |
P304 | page(s) | 15293 | |
P577 | publication date | 2017-05-10 | |
P1433 | published in | Nature Communications | Q573880 |
P1476 | title | Heterodimerization of Munc13 C2A domain with RIM regulates synaptic vesicle docking and priming | |
P478 | volume | 8 |
Q90061044 | A Hyperactive Form of unc-13 Enhances Ca2+ Sensitivity and Synaptic Vesicle Release Probability in C. elegans |
Q98209033 | A Trio of Active Zone Proteins Comprised of RIM-BPs, RIMs, and Munc13s Governs Neurotransmitter Release |
Q64072801 | Autaptic cultures of human induced neurons as a versatile platform for studying synaptic function and neuronal morphology |
Q41536357 | CAPS-1 requires its C2, PH, MHD1 and DCV domains for dense core vesicle exocytosis in mammalian CNS neurons |
Q52341087 | CSI1, PATROL1, and exocyst complex cooperate in delivery of cellulose synthase complexes to the plasma membrane. |
Q53840590 | ELKS active zone proteins as multitasking scaffolds for secretion. |
Q55313799 | Ethanol Regulates Presynaptic Activity and Sedation through Presynaptic Unc13 Proteins in Drosophila. |
Q42380467 | Frequency-dependent mobilization of heterogeneous pools of synaptic vesicles shapes presynaptic plasticity. |
Q89921518 | Functions of Vertebrate Ferlins |
Q64104459 | Heterodimerization of UNC-13/RIM regulates synaptic vesicle release probability but not priming in |
Q57173506 | Mechanism of neurotransmitter release coming into focus |
Q64087085 | Membrane bridging by Munc13-1 is crucial for neurotransmitter release |
Q61813220 | Multiple factors maintain assembled trans-SNARE complexes in the presence of NSF and αSNAP |
Q47398975 | Munc13 proteins control regulated exocytosis in mast cells |
Q38628008 | Neurosecretion: what can we learn from chromaffin cells |
Q52614917 | RIM C2B Domains Target Presynaptic Active Zone Functions to PIP2-Containing Membranes. |
Q83229182 | RIM-BP2 primes synaptic vesicles recruitment of Munc13-1 at hippocampal mossy fiber synapses |
Q64058070 | Rapid active zone remodeling consolidates presynaptic potentiation |
Q61806540 | SNARE machinery is optimized for ultrafast fusion |
Q92916397 | The exocyst complex and Rab5 are required for abscission by localizing ESCRT III subunits to the cytokinetic bridge |
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